EE200100382A - Ras-farnesüültransferaasi inhibiitori ja sulfobutüüleeter-7-ß-tsüklodekstriini või 2-hüdroksüpropüül-ß-tsüklodekstriini kompleks ja selle valmistamise meetod - Google Patents

Ras-farnesüültransferaasi inhibiitori ja sulfobutüüleeter-7-ß-tsüklodekstriini või 2-hüdroksüpropüül-ß-tsüklodekstriini kompleks ja selle valmistamise meetod

Info

Publication number
EE200100382A
EE200100382A EEP200100382A EEP200100382A EE200100382A EE 200100382 A EE200100382 A EE 200100382A EE P200100382 A EEP200100382 A EE P200100382A EE P200100382 A EEP200100382 A EE P200100382A EE 200100382 A EE200100382 A EE 200100382A
Authority
EE
Estonia
Prior art keywords
cyclodextrin
ras
hydroxypropyl
complex
preparation
Prior art date
Application number
EEP200100382A
Other languages
English (en)
Estonian (et)
Inventor
S. Raghavan Krishnaswamy
M. Malloy Timothy
A. Varia Sailesh
Original Assignee
Bristol-Myers Squibb Company
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Bristol-Myers Squibb Company filed Critical Bristol-Myers Squibb Company
Publication of EE200100382A publication Critical patent/EE200100382A/xx

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/551Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
    • A61K31/55131,4-Benzodiazepines, e.g. diazepam or clozapine
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y5/00Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/50Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates
    • A61K47/69Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit
    • A61K47/6949Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit inclusion complexes, e.g. clathrates, cavitates or fullerenes
    • A61K47/6951Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the conjugate being characterised by physical or galenical forms, e.g. emulsion, particle, inclusion complex, stent or kit inclusion complexes, e.g. clathrates, cavitates or fullerenes using cyclodextrin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nanotechnology (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • Medical Informatics (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Biophysics (AREA)
  • Biotechnology (AREA)
  • General Engineering & Computer Science (AREA)
  • Molecular Biology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Polysaccharides And Polysaccharide Derivatives (AREA)
  • Plural Heterocyclic Compounds (AREA)
EEP200100382A 1999-01-21 1999-12-21 Ras-farnesüültransferaasi inhibiitori ja sulfobutüüleeter-7-ß-tsüklodekstriini või 2-hüdroksüpropüül-ß-tsüklodekstriini kompleks ja selle valmistamise meetod EE200100382A (et)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US11664799P 1999-01-21 1999-01-21
PCT/US1999/030424 WO2000042849A1 (en) 1999-01-21 1999-12-21 COMPLEX OF RAS-FARNESYLTRANSFERASE INHIBITOR AND SULFOBUTYLETHER-7-β-CYCLODEXTRIN OR 2-HYDROXYPROPYL-β-CYCLODEXTRIN AND METHOD

Publications (1)

Publication Number Publication Date
EE200100382A true EE200100382A (et) 2002-12-16

Family

ID=22368422

Family Applications (1)

Application Number Title Priority Date Filing Date
EEP200100382A EE200100382A (et) 1999-01-21 1999-12-21 Ras-farnesüültransferaasi inhibiitori ja sulfobutüüleeter-7-ß-tsüklodekstriini või 2-hüdroksüpropüül-ß-tsüklodekstriini kompleks ja selle valmistamise meetod

Country Status (33)

Country Link
US (1) US6218375B1 (id)
EP (1) EP1143796A4 (id)
JP (1) JP2002535253A (id)
KR (1) KR100708360B1 (id)
CN (1) CN1219517C (id)
AR (1) AR022323A1 (id)
AU (1) AU772204B2 (id)
BG (1) BG105666A (id)
BR (1) BR9916566A (id)
CA (1) CA2359646C (id)
CO (1) CO5160253A1 (id)
CZ (1) CZ20012601A3 (id)
EE (1) EE200100382A (id)
GE (1) GEP20043214B (id)
HK (1) HK1038865A1 (id)
HU (1) HUP0105160A3 (id)
ID (1) ID30139A (id)
IL (1) IL144025A (id)
LT (1) LT4893B (id)
LV (1) LV12712B (id)
MY (1) MY119700A (id)
NO (1) NO20013585L (id)
NZ (1) NZ511995A (id)
PE (1) PE20001419A1 (id)
PL (1) PL195280B1 (id)
RU (1) RU2230062C2 (id)
SK (1) SK9602001A3 (id)
TR (1) TR200102109T2 (id)
TW (1) TWI232752B (id)
UA (1) UA67825C2 (id)
UY (2) UY25987A1 (id)
WO (1) WO2000042849A1 (id)
ZA (1) ZA200104416B (id)

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US20100204178A1 (en) 2006-10-02 2010-08-12 James Cloyd Novel parenteral carbamazepine formulation
CN100503647C (zh) * 2005-11-02 2009-06-24 南京师范大学 羟丙基-磺丁基-β-环糊精及其制备方法、分析方法以及在药学上的应用
TW200806284A (en) * 2006-03-31 2008-02-01 Alcon Mfg Ltd Prenyltransferase inhibitors for ocular hypertension control and the treatment of glaucoma
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US12370352B2 (en) 2007-06-28 2025-07-29 Cydex Pharmaceuticals, Inc. Nasal and ophthalmic delivery of aqueous corticosteroid solutions
MY169791A (en) 2008-10-22 2019-05-15 Array Biopharma Inc Substituted pyrazolo [1,5-a] pyrimidine compounds as trk kinase inhibitors
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ES2642843T3 (es) * 2011-10-07 2017-11-20 Pisces Therapeutics Llc Tratamiento de enfermedad maligna y no maligna con antagonistas de Ras
CN105194685A (zh) * 2015-10-15 2015-12-30 重庆大学 磺胺脒的磺丁基醚-β-环糊精包合物及其粉针制剂
EP3389653B1 (en) 2015-12-16 2023-11-08 Neurophyxia B.V. 2-iminobiotin for use in the treatment of brain cell injury
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JOP20190092A1 (ar) 2016-10-26 2019-04-25 Array Biopharma Inc عملية لتحضير مركبات بيرازولو[1، 5-a]بيريميدين وأملاح منها
US20210145816A1 (en) * 2019-11-15 2021-05-20 Cyclolab Cyclodextrin Research And Development Laboratory Ltd. Pharmaceutical formulation of lonafarnib with a sulfobutylether beta-cyclodextrin
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AU2024360465A1 (en) 2023-10-12 2026-04-09 Revolution Medicines, Inc. Macrocyclic ras inhibitors
WO2025171296A1 (en) 2024-02-09 2025-08-14 Revolution Medicines, Inc. Ras inhibitors
TW202547461A (zh) 2024-05-17 2025-12-16 美商銳新醫藥公司 Ras抑制劑
WO2025255438A1 (en) 2024-06-07 2025-12-11 Revolution Medicines, Inc. Methods of treating a ras protein-related disease or disorder
WO2025265060A1 (en) 2024-06-21 2025-12-26 Revolution Medicines, Inc. Therapeutic compositions and methods for managing treatment-related effects
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Also Published As

Publication number Publication date
UY25987A1 (es) 2000-09-29
ID30139A (id) 2001-11-08
AU2374000A (en) 2000-08-07
CN1219517C (zh) 2005-09-21
NO20013585L (no) 2001-09-04
BG105666A (en) 2002-04-30
NO20013585D0 (no) 2001-07-20
KR20010101611A (ko) 2001-11-14
AR022323A1 (es) 2002-09-04
HUP0105160A2 (hu) 2002-05-29
RU2230062C2 (ru) 2004-06-10
MY119700A (en) 2005-06-30
EP1143796A1 (en) 2001-10-17
PL366338A1 (en) 2005-01-24
WO2000042849A1 (en) 2000-07-27
CZ20012601A3 (cs) 2002-05-15
LT2001064A (en) 2001-10-25
UY25986A1 (es) 2000-09-29
PE20001419A1 (es) 2001-02-21
LV12712B (en) 2002-01-20
JP2002535253A (ja) 2002-10-22
UA67825C2 (uk) 2004-07-15
ZA200104416B (en) 2002-05-29
IL144025A0 (en) 2002-04-21
LV12712A (lv) 2001-09-20
US6218375B1 (en) 2001-04-17
HUP0105160A3 (en) 2003-01-28
BR9916566A (pt) 2001-11-13
CA2359646C (en) 2008-12-02
CO5160253A1 (es) 2002-05-30
LT4893B (lt) 2002-02-25
TWI232752B (en) 2005-05-21
IL144025A (en) 2004-05-12
SK9602001A3 (en) 2002-06-04
HK1038865A1 (zh) 2002-04-04
KR100708360B1 (ko) 2007-04-17
GEP20043214B (en) 2004-04-26
CA2359646A1 (en) 2000-07-27
PL195280B1 (pl) 2007-08-31
EP1143796A4 (en) 2002-03-20
TR200102109T2 (tr) 2001-12-21
NZ511995A (en) 2003-11-28
CN1333651A (zh) 2002-01-30
AU772204B2 (en) 2004-04-22

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